CN114450343A

CN114450343A - Thermoplastic resin composition and molded article thereof

Info

Publication number: CN114450343A
Application number: CN202080065079.XA
Authority: CN
Inventors: 任晟午; 秋东辉
Original assignee: Lotte Chemical Corp
Current assignee: Lotte Chemical Corp
Priority date: 2019-10-30
Filing date: 2020-09-09
Publication date: 2022-05-06
Anticipated expiration: 2040-09-09
Also published as: CN114450343B; US20220251348A1; WO2021085840A1; KR20210051231A; KR102412172B1

Abstract

The thermoplastic resin composition according to the present invention is characterized by comprising: about 100 parts by weight of a rubber-modified aromatic vinyl copolymer resin; about 6 to about 35 parts by weight of a propylene-ethylene random copolymer resin; about 3 to about 10 parts by weight of a styrene-butadiene rubber polymer; and about 1 to about 10 parts by weight of an ethylene-alpha-olefin rubber polymer. The thermoplastic resin composition has excellent impact resistance, hardness, heat resistance, chemical resistance and moldability.

Description

Thermoplastic resin composition and molded article thereof

Technical Field

The present invention relates to a thermoplastic resin composition and a molded article made therefrom. More particularly, the present invention relates to a thermoplastic resin composition exhibiting good characteristics in terms of impact resistance, rigidity, heat resistance, chemical resistance, moldability, etc., and a molded article made therefrom.

Background

Rubber-modified aromatic vinyl copolymer resins (such as acrylonitrile-butadiene-styrene copolymer resins (ABS resins) and the like) have good characteristics in terms of impact resistance, rigidity, heat resistance, chemical resistance, moldability and chemical resistance, relative to freon (CFC-11) used as a blowing agent for rigid polyurethane foams, and are applied to resins for refrigerators and the like.

However, since conventional foaming compounds including freon have been found to destroy the ozone layer, they have been replaced with eco-friendly foaming agents, such as Hydrofluoroolefin (HFO) foaming agents, which have very low Global Warming Potential (GWP) and Ozone Depletion Potential (ODP) and high foaming efficiency. Since such eco-friendly foaming agents exhibit stronger chemical corrosion than conventional foaming compounds, the eco-friendly foaming agents are required to have a higher level of chemical resistance than the resin for a refrigerator used therewith.

Polyolefin resins including polypropylene resins may be used as the resin for refrigerators to which the eco-friendly blowing agent is applied, due to advantages such as good chemical resistance, low specific gravity, and high price competitiveness. However, polyolefin resins have problems such as post shrinkage due to low heat resistance and hardness when polyurethane expands, and no contact with expanded polyurethane.

Although it is suggested to use a mixture of a polyolefin resin and a rubber-modified aromatic vinyl copolymer resin, there is a problem in that characteristics are deteriorated upon mixing due to lack of compatibility between the polyolefin resin and the rubber-modified aromatic vinyl copolymer resin.

Therefore, there is a need to develop a thermoplastic resin composition that exhibits good characteristics in terms of impact resistance, rigidity, heat resistance, chemical resistance, moldability, and the like, without these problems.

The background art of the present invention is disclosed in korean patent laid-open publication No. 10-2009-0073453 and the like.

Disclosure of Invention

An object of the present invention is to provide a thermoplastic resin composition having good characteristics in terms of impact resistance, rigidity, heat resistance, chemical resistance, moldability, and the like.

It is another object of the present invention to provide a molded article made of the thermoplastic resin composition.

The above and other objects of the present invention can be accomplished by the present invention described below.

1. One aspect of the present invention relates to a thermoplastic resin composition. The thermoplastic resin composition comprises: about 100 parts by weight of a rubber-modified aromatic vinyl copolymer resin; about 6 to about 35 parts by weight of a propylene-ethylene random copolymer resin; about 3 to about 10 parts by weight of a styrene-butadiene rubber polymer; and about 1 to about 10 parts by weight of an ethylene-alpha-olefin rubber polymer.

2. In embodiment 1, the rubber-modified aromatic vinyl copolymer resin may include a rubber-modified vinyl graft copolymer and an aromatic vinyl copolymer resin.

3. In embodiment 1 or 2, the rubber-modified vinyl graft copolymer may be prepared by graft-polymerizing a monomer mixture including an aromatic vinyl monomer and a vinyl cyanide monomer with a rubber polymer.

4. In embodiments 1 to 3, the propylene-ethylene random copolymer resin may be a polymer of a monomer mixture including about 90% by weight to about 99% by weight of propylene and about 1% by weight to about 10% by weight of ethylene.

5. In embodiments 1 to 4, the propylene-ethylene random copolymer resin may have a melt flow index (MI) of about 1g/10min to about 10g/10min, measured at 230 ℃ and 2.16kgf according to ASTM D1238.

6. In embodiments 1 to 5, the styrene-butadiene rubber polymer may be a polymer of a monomer mixture including about 25 wt% to about 45 wt% of styrene and about 55 wt% to about 75 wt% of butadiene.

7. In embodiments 1 to 6, the ethylene- α -olefin rubber polymer may be a polymer of a monomer mixture including about 25% to about 55% by weight of ethylene and about 45% to about 75% by weight of an α -olefin.

8. In embodiments 1 to 7, the propylene-ethylene random copolymer resin and the styrene-butadiene rubber polymer may be present in a weight ratio of about 2:1 to about 4: 1.

9. In embodiments 1 through 8, the styrene-butadiene rubber polymer and the ethylene-a-olefin rubber polymer may be present in a weight ratio of 1:1 to about 3: 1.

10. In embodiments 1 to 9, the thermoplastic resin composition may have a notched Izod impact strength of about 13kgf cm/cm to about 25kgf cm/cm as measured on a 1/4 ″ thick sample according to ASTM D256.

11. In embodiments 1 to 10, the thermoplastic resin composition may have about 250kgf/cm as measured on a 3.2mm thick sample at 5mm/min according to ASTM D638²To about 400kgf/cm²The tensile strength of (2).

12. In embodiments 1 to 11, the thermoplastic resin composition may have a vicat softening temperature of about 80 ℃ to about 95 ℃ as measured at 50 ℃/hour under a load of 5kgf according to ISO R306.

13. In embodiments 1 to 12, after a sample having a size of 200mm × 50mm × 2mm is mounted on an 1/4 oval jig (major axis length: 120mm, minor axis length: 34mm), completely coated with 10ml of olive oil, and left to stand for 24 hours, the thermoplastic resin composition may have a cracking strain (∈) of about 1% to about 1.2%, calculated on the sample according to equation 1:

[ equation 1]

Where ε represents the cracking strain, a represents the length of the major axis of the elliptical fixture (mm), b represents the length of the minor axis of the elliptical fixture (mm), t represents the thickness of the sample (mm), and x represents the distance from the perpendicular intersection between the location where cracking occurred and the major axis of the elliptical fixture to the center point of the elliptical fixture.

14. In embodiments 1 to 13, the dimensions are 65mm × 3.2mm (length × thickness)) After aging the sample in the chamber at 130 ℃ for 5min, the thermoplastic resin composition may have about 10kgf/cm as measured at 150mm/min according to ASTM D638²To about 20kgf/cm²High temperature tensile strength.

15. Another aspect of the invention relates to a molded article. The molded article is made of the thermoplastic resin composition according to any one of embodiments 1 to 14.

The present invention provides a thermoplastic resin composition having good characteristics in terms of impact resistance, rigidity, heat resistance, chemical resistance, moldability, etc., and a molded article made therefrom.

Detailed Description

Hereinafter, embodiments of the present invention will be described in detail.

The thermoplastic resin composition according to the present invention comprises: (A) a rubber-modified aromatic vinyl copolymer resin; (B) a propylene-ethylene random copolymer resin; (C) styrene-butadiene rubber polymers; and (D) an ethylene-alpha-olefin rubber polymer.

As used herein, to indicate a specific numerical range, the expression "a to b" means ". gtoreq.a and. ltoreq.b".

(A) Rubber-modified aromatic vinyl copolymer resin

The rubber-modified aromatic vinyl copolymer resin according to one embodiment of the present invention may include (a1) a rubber-modified vinyl graft copolymer and (a2) an aromatic vinyl copolymer resin.

(A1) Rubber modified vinyl graft copolymers

The rubber-modified vinyl graft copolymer according to an embodiment of the present invention may be obtained by graft-polymerizing a monomer mixture including an aromatic vinyl monomer and a vinyl cyanide monomer with a rubber polymer. For example, the rubber-modified vinyl graft copolymer may be obtained by graft-polymerizing a monomer mixture including an aromatic vinyl monomer and a vinyl cyanide monomer with a rubber polymer, and, optionally, the monomer mixture may further include a monomer for imparting processability and heat resistance. Here, the polymerization may be performed by any suitable polymerization method known in the art, such as emulsion polymerization, suspension polymerization, and the like. Further, the rubber-modified vinyl graft copolymer may have a core (rubber polymer) -shell (copolymer of monomer mixture) structure, but is not limited thereto.

In some embodiments, the rubbery polymer may include diene rubbers (e.g., polybutadiene and poly (acrylonitrile-butadiene)), saturated rubbers obtained by adding hydrogen to diene rubbers, isoprene rubbers, C₂To C₁₀Alkyl (meth) acrylate rubber, C₂To C₁₀Copolymers of alkyl (meth) acrylate rubbers and styrene, and ethylene-propylene-diene terpolymers (EPDM), and the like. These may be used alone or as a mixture thereof. For example, the rubber polymer may include diene rubber, (meth) acrylate rubber, specifically including butadiene rubber, butyl acrylate rubber, and the like.

In some embodiments, the rubbery polymer (rubber particles) may have an average (z-average) particle size of about 0.05 μm to about 6 μm, for example, about 0.15 μm to about 4 μm, specifically about 0.25 μm to about 3.5 μm. Within this range, the thermoplastic resin composition may have good impact resistance and appearance characteristics. Here, the average (Z-average) particle diameter of the rubber polymer (rubber particles) can be measured in a latex state by a light scattering method. Specifically, the rubber polymer latex is filtered through a screen to remove coagulum generated in the polymerization process of the rubber polymer. Then, a mixed solution of 0.5g of the latex and 30ml of distilled water was put into a1,000 ml flask, and then the flask was sequentially filled with distilled water to prepare a sample. Then, 10ml of the sample was transferred to a quartz cell, and then the average particle diameter of the rubber polymer was measured using a light scattering particle analyzer (Malvern co., ltd., Nano-zs).

In some embodiments, the rubbery polymer may be present in an amount of about 20 wt% to about 80 wt%, for example, about 25 wt% to about 70 wt%, based on 100 wt% of the rubber modified vinyl graft copolymer, and the monomer mixture (including the aromatic vinyl monomer and the vinyl cyanide monomer) may be present in an amount of about 30 wt% to about 80 wt%, for example, about 40 wt% to about 75 wt%, based on 100 wt% of the rubber modified vinyl graft copolymer. Within this range, the thermoplastic resin composition may have good characteristics in terms of impact resistance, appearance characteristics, and the like.

In some embodiments, aromatic vinyl monomers may be graft copolymerized with the rubber polymer, and the aromatic vinyl monomers may include, for example, styrene, α -methylstyrene, β -methylstyrene, p-tert-butylstyrene, ethylstyrene, vinylxylene, monochlorostyrene, dichlorostyrene, dibromostyrene, vinylnaphthalene, and the like. These may be used alone or as a mixture thereof. The aromatic vinyl monomer may be present in an amount of about 10 wt% to about 90 wt%, for example, about 10 wt% to about 60 wt%, based on 100 wt% of the monomer mixture. Within this range, the thermoplastic resin composition may have good characteristics in terms of processability, impact resistance, and the like.

In some embodiments, the vinyl cyanide monomer is a monomer copolymerizable with the aromatic vinyl monomer, and the vinyl cyanide monomer may include, for example, acrylonitrile, methacrylonitrile, ethacrylonitrile, phenylacrylonitrile, α -chloroacrylonitrile, and fumaronitrile, but is not limited thereto. These may be used alone or as a mixture thereof. For example, the vinyl cyanide monomer may be acrylonitrile, methacrylonitrile, and the like. The vinyl cyanide monomer may be present in an amount of about 5 wt% to about 60 wt%, for example, about 10 wt% to about 50 wt%, based on 100 wt% of the monomer mixture. Within this range, the thermoplastic resin composition may have good characteristics in terms of chemical resistance, mechanical characteristics, and the like.

In some embodiments, monomers used to impart processability and heat resistance may include, for example, (meth) acrylic acid, C₁To C₁₀Alkyl (meth) acrylates, maleic anhydride and N-substituted maleimides, but are not limited thereto. 60 wt% or less, for example, about 1 wt% to about 50 wt%, based on 100 wt% of the monomer mixture. Within this range, the monomer for imparting processability and heat resistance can impart processability and heat resistance to the thermoplastic resin composition,while the other characteristics do not deteriorate.

In some embodiments, the rubber modified vinyl graft copolymer may include the following copolymers: a copolymer (g-ABS) obtained by grafting a styrene monomer as an aromatic vinyl compound and an acrylonitrile monomer as a vinyl cyanide compound to a butadiene rubber polymer, a copolymer (g-MBS) obtained by grafting a styrene monomer as an aromatic vinyl compound and methyl methacrylate as a monomer for imparting processability and heat resistance to a butadiene rubber polymer, a copolymer (g-MABS) obtained by grafting a styrene monomer, an acrylonitrile monomer and methyl methacrylate to a butadiene rubber polymer, and an acrylate-styrene-acrylonitrile graft copolymer (g-ASA) obtained by grafting a styrene monomer as an aromatic vinyl compound and an acrylonitrile monomer as a vinyl cyanide compound to a butyl acrylate rubber polymer, and the like.

In some embodiments, the rubber-modified vinyl graft copolymer may be present in an amount of about 20 to about 50 wt%, for example, about 25 to about 45 wt%, based on 100 wt% of the rubber-modified aromatic vinyl copolymer resin. Within this range, the thermoplastic resin composition may exhibit good characteristics in terms of impact resistance, flowability (molding processability), appearance characteristics, and balance therebetween.

(A2) Aromatic vinyl copolymer resin

The aromatic vinyl copolymer resin according to one embodiment of the present invention may include an aromatic vinyl copolymer resin used for a typical rubber-modified aromatic vinyl copolymer resin. For example, the aromatic vinyl copolymer resin may be a polymer of a monomer mixture including an aromatic vinyl monomer and a monomer copolymerizable with the aromatic vinyl monomer.

In some embodiments, the aromatic vinyl copolymer resin may be obtained by mixing an aromatic vinyl monomer with a monomer copolymerizable with the aromatic vinyl monomer, and then polymerizing the mixture. Here, the polymerization may be performed by any suitable polymerization method known in the art, such as emulsion polymerization, suspension polymerization, bulk polymerization, and the like.

In some embodiments, the aromatic vinyl monomers may include, but are not limited to, styrene, alpha-methylstyrene, beta-methylstyrene, p-tert-butylstyrene, ethylstyrene, vinylxylene, monochlorostyrene, dichlorostyrene, dibromostyrene, and vinylnaphthalene. These may be used alone or as a mixture thereof. The aromatic vinyl monomer may be present in an amount of about 10 to about 95 wt%, for example, about 20 to about 90 wt%, based on 100 wt% of the aromatic vinyl copolymer resin. Within this range, the thermoplastic resin composition may have good characteristics in terms of impact resistance, flowability, and the like.

In some embodiments, the monomer copolymerizable with the aromatic vinyl monomer may include a vinyl cyanide monomer and/or an alkyl (meth) acrylic monomer. For example, the monomer copolymerizable with the aromatic vinyl monomer may include a vinyl cyanide monomer, or a vinyl cyanide monomer and an alkyl (meth) acrylic monomer, and specifically may include a vinyl cyanide monomer and an alkyl (meth) acrylic monomer.

In some embodiments, the vinyl cyanide monomers may include acrylonitrile, methacrylonitrile, ethacrylonitrile, phenylacrylonitrile, alpha-chloroacrylonitrile, and fumaronitrile, but are not limited thereto. These may be used alone or as a mixture thereof. For example, the vinyl cyanide monomers may include acrylonitrile, methacrylonitrile, and the like.

In some embodiments, the alkyl (meth) acrylic monomer may include (meth) acrylic acid and/or C₁To C₁₀An alkyl methacrylate. These may be used alone or as a mixture thereof. For example, methyl methacrylate, methyl acrylate, and the like can be used.

The monomer copolymerizable with the aromatic vinyl monomer may be present in an amount of about 5 to about 90% by weight, for example, about 10 to about 80% by weight, based on 100% by weight of the aromatic vinyl copolymer resin. Within this range, the thermoplastic resin composition may have good characteristics in terms of impact resistance, flowability, and the like.

In some embodiments, the aromatic vinyl copolymer resin may have a weight average molecular weight (Mw) of about 10,000g/mol to about 300,000g/mol, for example, about 15,000g/mol to about 150,000g/mol, as measured by Gel Permeation Chromatography (GPC). Within this range, the thermoplastic resin composition may have good mechanical strength, moldability, and the like.

In some embodiments, the aromatic vinyl copolymer resin may be present in an amount of about 50 to about 90 wt%, for example, about 55 to about 85 wt%, based on 100 wt% of the rubber-modified aromatic vinyl copolymer resin. Within this range, the thermoplastic resin composition can exhibit good characteristics in terms of impact resistance, flowability (molding processability), and the like.

(B) Propylene-ethylene random copolymer resin

According to the present invention, the propylene-ethylene random copolymer resin is used to improve chemical resistance (oil resistance), moldability, and the like of the thermoplastic resin composition, and may be an amorphous or low-crystalline propylene-ethylene random copolymer resin.

In some embodiments, the propylene-ethylene random copolymer resin may be a polymer of a monomer mixture including about 90% to about 99% (e.g., about 94 to about 97%) by weight of propylene and about 1% to about 10% (e.g., about 3% to about 6%) by weight of ethylene. Within this range, the thermoplastic resin composition can exhibit good chemical resistance (oil resistance), good moldability, and the like.

In some embodiments, the propylene-ethylene random copolymer resin may have a melt flow index (MI) of about 1g/10min to about 10g/10min, for example, about 1g/10min to about 5g/10, as measured at 230 ℃ and 2.16kgf according to ASTM D1238. Within this range, the thermoplastic resin composition can exhibit good chemical resistance (oil resistance), good moldability, and the like.

In some embodiments, the propylene-ethylene random copolymer resin may be present in an amount of about 6 parts by weight to about 35 parts by weight, for example, about 10 parts by weight to about 30 parts by weight, relative to about 100 parts by weight of the rubber-modified aromatic vinyl copolymer resin. If the content of the propylene-ethylene random copolymer resin is less than about 6 parts by weight, the thermoplastic resin composition may suffer from deterioration in chemical resistance (oil resistance) and the like, and if the content of the propylene-ethylene random copolymer resin exceeds about 35 parts by weight, the thermoplastic resin composition may suffer from deterioration in compatibility, moldability, rigidity and the like.

(C) Styrene-butadiene rubber polymer

According to the present invention, the styrene-butadiene rubber polymer is used to improve the compatibility of the rubber-modified aromatic vinyl copolymer resin and the propylene-ethylene random copolymer resin, while improving the impact resistance, rigidity, and the like of the thermoplastic resin composition together with the ethylene- α -olefin rubber polymer.

In some embodiments, the styrene-butadiene rubber polymer may be a polymer of a monomer mixture including about 25% to about 45% (e.g., about 25% to about 35%) by weight styrene and about 55% to about 75% (e.g., about 60% to about 70%) by weight butadiene. Within this range, the thermoplastic resin composition may exhibit good impact resistance and good rigidity.

In some embodiments, the styrene-butadiene rubber polymer may have a melt flow index (MI) of about 1g/10min to about 10g/10min, for example, about 3g/10min to about 8g/10min, as measured at 200 ℃ and 5kgf according to ASTM D1238. Within this range, the thermoplastic resin composition may exhibit good impact resistance and good rigidity.

In some embodiments, the styrene-butadiene rubber polymer may be present in an amount of about 3 parts by weight to about 10 parts by weight, for example, about 4 parts by weight to about 7 parts by weight, relative to about 100 parts by weight of the rubber-modified aromatic vinyl copolymer resin. If the content of the styrene-butadiene rubber polymer is less than about 3 parts by weight, the thermoplastic resin composition may be deteriorated in impact resistance, rigidity, compatibility, and the like, and if the content of the styrene-butadiene rubber polymer exceeds about 10 parts by weight, the thermoplastic resin composition may be deteriorated in rigidity, and the like.

In some embodiments, the propylene-ethylene random copolymer resin (B) and the styrene-butadiene rubber polymer (C) may be present in a weight ratio (B: C) of about 2:1 to about 4:1, for example, about 2:1 to about 3: 1. Within this range, the thermoplastic resin composition may exhibit good characteristics in terms of impact resistance, rigidity, compatibility, and the like.

(D) Ethylene-alpha-olefin rubber polymer

According to the present invention, the ethylene- α -olefin rubber polymer is used to improve the compatibility of the rubber-modified aromatic vinyl copolymer resin with the propylene-ethylene random copolymer resin, while improving the impact resistance, rigidity, and the like of the thermoplastic resin composition together with the styrene-butadiene rubber polymer.

In some embodiments, the ethylene-a-olefin rubber polymer may be a polymer of a monomer mixture including about 25% to about 55% (e.g., about 30% to about 50%) by weight ethylene and about 45% to about 75% (e.g., about 50% to about 70%) by weight a-olefin. Within this range, the thermoplastic resin composition may exhibit good impact resistance and good rigidity.

In some embodiments, the ethylene-a-olefin rubber polymer may include at least one of an ethylene-1-octene copolymer, an ethylene-1-butene copolymer, an ethylene-1-pentene copolymer, an ethylene-1-hexene copolymer, an ethylene-1-heptene copolymer, an ethylene-1-decene copolymer, an ethylene-1-undecene copolymer, and an ethylene-1-dodecene copolymer.

In some embodiments, the ethylene-alpha-olefin rubber polymer may have a specific gravity of from about 0.85 to about 0.88, e.g., from about 0.86 to about 0.87, as measured in accordance with ASTM D792, and a melt flow index (MI), as measured in accordance with ASTM D1238 at 190 ℃ and 2.16kgf, of from about 0.5g/10min to about 5g/10min, e.g., from about 0.5g/10min to about 2g/10 min. Within this range, the thermoplastic resin composition may exhibit good impact resistance and good rigidity.

In some embodiments, the ethylene-a-olefin rubber polymer may be present in an amount of about 1 part by weight to about 10 parts by weight, for example, about 2 parts by weight to about 8 parts by weight, relative to about 100 parts by weight of the rubber-modified aromatic vinyl copolymer resin. If the content of the ethylene- α -olefin rubber polymer is less than about 2 parts by weight, the thermoplastic resin composition may suffer from deterioration in impact resistance and the like, and if the content of the ethylene- α -olefin rubber polymer exceeds about 10 parts by weight, the thermoplastic resin composition may suffer from deterioration in rigidity, heat resistance and the like.

In some embodiments, the styrene-butadiene rubber polymer (C) and the ethylene-a-olefin rubber polymer (D) may be present in a weight ratio (C: D) of about 1:1 to about 3:1, for example, about 1.5:1 to about 2: 1. Within this range, the thermoplastic resin composition may exhibit good impact resistance and good rigidity.

According to an embodiment of the present invention, the thermoplastic resin composition may further include an additive used for typical thermoplastic resin compositions. Examples of the additives may include inorganic fillers, flame retardants, anti-dripping agents, antioxidants, lubricants, mold release agents, nucleating agents, stabilizers, pigments, dyes, and mixtures thereof, but are not limited thereto. The additive may be present in an amount of about 0.001 parts by weight to about 40 parts by weight, for example, about 0.1 parts by weight to about 10 parts by weight, relative to about 100 parts by weight of the rubber-modified aromatic vinyl copolymer resin.

The thermoplastic resin composition according to one embodiment of the present invention may be prepared in the form of pellets by mixing the aforementioned components, followed by melt extrusion at about 180 ℃ to about 260 ℃, for example, about 200 ℃ to about 250 ℃ using a typical double-rod extruder.

In some embodiments, the thermoplastic resin composition may have a dispersion of a rubber-modified aromatic vinyl copolymer resin and an ethylene- α -olefin rubber polymer, the dispersion being present in a continuous phase of the propylene-ethylene random copolymer resin, wherein the styrene-butadiene rubber polymer may be present at an interface between the propylene-ethylene random copolymer resin and the rubber-modified aromatic vinyl copolymer resin.

In some embodiments, the thermoplastic resin composition may have a notched Izod impact strength of from about 13 kgf-cm/cm to about 25 kgf-cm/cm, for example, from about 13 kgf-cm/cm to about 20 kgf-cm/cm, as measured on a 1/4 "thick sample according to ASTM D256.

In some embodiments, the thermoplastic resin composition may have a thickness of about 250kgf/cm as measured at 5mm/min for a 3.2mm thick sample according to ASTM D638²To about 400kgf/cm²Tensile strength of (2), e.g., about 250kgf/cm²To about 350kgf/cm²。

In some embodiments, the thermoplastic resin composition may have a vicat softening temperature of about 80 ℃ to about 95 ℃, for example, about 85 ℃ to about 95 ℃, measured at 50 ℃/hour under a load of 5kgf according to ISO R306.

In some embodiments, after a sample having a size of 200mm × 50mm × 2mm is mounted on an 1/4 oval jig (major axis length: 120mm, minor axis length: 34mm), completely coated with 10ml of olive oil, and left to stand for 24 hours, the thermoplastic resin composition may have a cracking strain (∈) of about 1% to about 1.2%, for example, about 1.04% to about 1.16%, calculated on the sample according to equation 1.

[ equation 1]

In some embodiments, the thermoplastic resin composition may have about 10kgf/cm after aging a sample having dimensions of 65mm x 3.2mm (length x thickness) in a chamber at 130 ℃ for 5min, measured at 150mm/min according to ASTM D638²To about 20kgf/cm²High temperature tensile strength of, for example, about 10kgf/cm²To about 15kgf/cm²。

The molded article according to the present invention is made of the thermoplastic resin composition set forth above. The thermoplastic resin composition may be prepared in the form of pellets. The prepared pellets can be made into various molded articles (products) by various molding methods such as injection molding, extrusion molding, vacuum molding and casting. These molding methods are well known to those skilled in the art. The molded article can be made by vacuum molding and has good characteristics in terms of impact resistance, rigidity, heat resistance, chemical resistance (oil resistance), moldability and a balance therebetween, and can be effectively used for interior and exterior materials of refrigerators.

In some embodiments, the molded article may be a material within a refrigerator in contact with an expansion layer that may be expanded with HFO (hydrofluoroolefin) or freon.

Next, the present invention will be described in more detail with reference to some examples. It should be understood that these examples are provided for illustration only and are in no way to be construed as limiting the invention.

Examples

The details of the components used in the examples and comparative examples are as follows.

(A) Rubber-modified aromatic vinyl copolymer resin

A mixture of 25% by weight of (a1) rubber-modified vinyl graft copolymer and 75% by weight of (a2) aromatic vinyl copolymer resin was used.

(A1) Rubber modified vinyl graft copolymers

g-ABS prepared by graft copolymerizing styrene and acrylonitrile (weight ratio: 75/25) with 55% by weight of a butadiene rubber having an average particle size of 0.3 μm was used.

(A2) Aromatic vinyl copolymer resin

SAN resin (weight average molecular weight: 140,000g/mol) prepared by polymerizing 80% by weight of styrene and 20% by weight of acrylonitrile was used.

(B1) An ethylene-propylene random copolymer resin (manufacturer: Lotte Chemical Co., Ltd., product name: SB-520, melt flow index 1.8g/10min) was used.

(B2) Polypropylene resin (manufacturer: lot Chemical co., ltd., product name: H1500) was used.

(B3) An ethylene-propylene block copolymer resin (manufacturer: Lotte Chemical Co., Ltd., product name: JH-370A) was used.

(C1) Styrene-butadiene rubber polymer (SBR, manufacturer: Kumho Petrochemical Co., Ltd., product name: KTR-201, styrene content: 31.5 wt%) was used.

(C2) Styrene-ethylene-butadiene-styrene copolymer (SEBS, manufacturer: KRATON, product name: G1652) was used.

(D1) As the ethylene-alpha-olefin rubber polymer, an ethylene-1-octene rubber polymer (EOR, manufacturer: DOW, product name: ENGAGE8150) was used.

(D2) Maleic anhydride grafted ethylene-octene rubber (EOR-g-MA, manufacturer: Useung Chemical Co., Ltd., product name: SP2000S) was used.

Examples 1 to 7 and comparative examples 1 to 10

The above components were mixed in the amounts listed in table 1, table 2 and table 3, and extruded at 200 ℃, thereby preparing pellets. Here, extrusion was performed using a twin-screw extruder (L/D-36,. phi.: 45mm), and the prepared pellets were dried at 80 ℃ for 4 hours or more and injection-molded in an injection molding machine of 6oz (molding temperature: 230 ℃, mold temperature: 60 ℃), thereby preparing samples. The following characteristics of the samples were evaluated by the following methods, and the results are shown in table 1, table 2, and table 3.

Measurement of properties

(1) Notched Izod impact strength (kgf. cm/cm): notched Izod impact strength was measured according to ASTM D256 on 1/4 "thick samples.

(2) Tensile Strength (TS, Unit: kgf/cm)²): tensile strength was measured on 3.2mm thick samples at 5mm/min according to ASTM D638.

(3) Vicat softening temperature (VST, unit:. degree. C.): the Vicat softening temperature was measured at 50 ℃/hour under a load of 5kgf according to ISO R306.

(4) Cracking strain (. epsilon., unit:%): after a sample having a size of 200mm × 50mm × 2mm was mounted on an 1/4 oval jig (major axis length: 120mm, minor axis length: 34mm), completely coated with 10ml of olive oil, and left for 24 hours, the sample was subjected to calculation of cracking strain according to equation 1.

[ equation 1]

(5) High temperature tensile Strength (Unit: kgf/cm)²): after aging a sample having dimensions of 65mm × 3.2mm (length × thickness) in a chamber at 130 ℃ for 5min, the high temperature tensile strength was measured on the sample at 150mm/min according to ASTM D638.

[ Table 1]

[ Table 2]

[ Table 3]

As can be seen from the above results, the thermoplastic resin composition according to the present invention exhibits good characteristics in terms of impact resistance (notched izod impact strength), rigidity (tensile strength), heat resistance (vicat softening temperature), chemical resistance (crack strain), moldability (high-temperature tensile strength), and the like.

In contrast, it can be seen that, as prepared in comparative example 1 in which the polypropylene resin (B2) was used instead of the ethylene-propylene random copolymer resin (B1), the thermoplastic resin composition suffered deterioration in impact resistance, moldability, and the like; as prepared in comparative example 2 in which the ethylene-propylene block copolymer resin (B3) was used instead of the ethylene-propylene random copolymer resin (B1), the thermoplastic resin composition suffered deterioration in moldability or the like; as prepared in comparative example 3 in which the content of the ethylene-propylene random copolymer resin was insufficient, the thermoplastic resin composition underwent deterioration in chemical resistance and the like; also, as prepared in comparative example 4 in which the content of the ethylene-propylene random copolymer resin was excessive, the thermoplastic resin composition suffered deterioration in heat resistance, rigidity, and the like. It can be seen that, as prepared in comparative example 5 in which a styrene-ethylene-butadiene-styrene copolymer (C2) was used instead of the styrene-butadiene rubber polymer (C1), the thermoplastic resin composition suffered deterioration in impact resistance, compatibility, and the like; as prepared in comparative example 6 in which the content of the styrene-butadiene rubber polymer is insufficient, the thermoplastic resin composition suffers deterioration in impact resistance, compatibility, and the like; and as prepared in comparative example 7 in which the content of the styrene-butadiene rubber polymer was excessive, the thermoplastic resin composition suffered deterioration in heat resistance, rigidity, and the like. In addition, it can be seen that, as prepared in comparative example 8 in which the maleic anhydride-grafted ethylene-octene rubber (D2) was used instead of the ethylene-1-octene rubber polymer (D1), the thermoplastic resin composition suffered deterioration in impact resistance and the like; as prepared in comparative example 9 in which the ethylene-1-octene rubber polymer was insufficient, the thermoplastic resin composition suffered deterioration in impact resistance and the like; also, as prepared in comparative example 10 in which the ethylene-1-octene rubber polymer was excessive, the thermoplastic resin composition suffered deterioration in heat resistance, rigidity, and the like.

It is to be understood that various modifications, alterations, changes and equivalent implementations may be made by those skilled in the art without departing from the spirit and scope of the invention.

Claims

1. A thermoplastic resin composition comprising:

about 100 parts by weight of a rubber-modified aromatic vinyl copolymer resin;

about 6 to about 35 parts by weight of a propylene-ethylene random copolymer resin;

about 3 to about 10 parts by weight of a styrene-butadiene rubber polymer; and

about 1 to about 10 parts by weight of an ethylene-alpha-olefin rubber polymer.

2. The thermoplastic resin composition of claim 1, wherein said rubber-modified aromatic vinyl copolymer resin comprises a rubber-modified vinyl graft copolymer and an aromatic vinyl copolymer resin.

3. The thermoplastic resin composition of claim 2, wherein said rubber-modified vinyl graft copolymer is prepared by graft-polymerizing a monomer mixture comprising an aromatic vinyl monomer and a vinyl cyanide monomer with a rubber polymer.

4. The thermoplastic resin composition of claim 1, wherein said propylene-ethylene random copolymer resin is a polymer of a monomer mixture comprising about 90 to about 99 wt% of propylene and about 1 to about 10 wt% of ethylene.

5. The thermoplastic resin composition of claim 1, wherein said propylene-ethylene random copolymer resin has a melt flow index (MI) of about 1g/10min to about 10g/10min, measured at 230 ℃ and 2.16kgf according to ASTM D1238.

6. The thermoplastic resin composition of claim 1, wherein said styrene-butadiene rubber polymer is a polymer of a monomer mixture comprising about 25 to about 45 wt.% styrene and about 55 to about 75 wt.% butadiene.

7. The thermoplastic resin composition of claim 1, wherein said ethylene-a-olefin rubber polymer is a polymer of a monomer mixture comprising about 25 to about 55 wt% ethylene and about 45 to about 75 wt% a-olefin.

8. The thermoplastic resin composition of claim 1, wherein said propylene-ethylene random copolymer resin and said styrene-butadiene rubber polymer are present in a weight ratio of about 2:1 to about 4: 1.

9. The thermoplastic resin composition of claim 1, wherein said styrene-butadiene rubber polymer and said ethylene-a-olefin rubber polymer are present in a weight ratio of about 1:1 to about 3: 1.

10. The thermoplastic resin composition of claim 1, wherein said thermoplastic resin composition has a notched izod impact strength of about 13 kgf-cm/cm to about 25 kgf-cm/cm as measured on a 1/4 "thick sample according to ASTM D256.

11. The thermoplastic resin composition of claim 1, wherein said thermoplastic resin composition has about 250kgf/cm, as measured at 5mm/min for a 3.2mm thick sample according to ASTM D638²To about 400kgf/cm²The tensile strength of (2).

12. The thermoplastic resin composition of claim 1, wherein said thermoplastic resin composition has a vicat softening temperature of about 80 ℃ to about 95 ℃ measured at 50 ℃/hour under a load of 5kgf in accordance with ISO R306.

13. The thermoplastic resin composition of claim 1, wherein after a sample having a size of 200mm x 50mm x 2mm is mounted on an 1/4 oval jig (major axis length: 120mm, minor axis length: 34mm), completely coated with 10ml of olive oil, and left to stand for 24 hours, the sample has a cracking strain(s) of about 1% to about 1.2%, calculated according to equation 1:

[ equation 1]

Where ε represents the cracking strain, a represents the major axis length (mm) of the elliptical fixture, b represents the minor axis length (mm) of the elliptical fixture, t represents the thickness (mm) of the sample, and x represents the distance from the perpendicular intersection between the location where cracking occurred and the major axis of the elliptical fixture to the center point of the elliptical fixture.

14. The thermoplastic resin composition of claim 1, wherein said thermoplastic resin composition has about 10kgf/cm after aging a sample having dimensions of 65mm x 3.2mm (length x thickness) in a chamber at 130 ℃ for 5 minutes, measured at 150mm/min according to ASTM D638²To about 20kgf/cm²High temperature tensile strength.

15. A molded article made of the thermoplastic resin composition according to any one of claims 1 to 14.